Nordic Regulatory Specialist

Ferring Pharmaceuticals

Kastrup, Denmark
Onsite
Nordic pharmaceutical industry experience
Regulatory affairs management
Marketing authorizations maintenance
Ferring Pharmaceuticals is seeking a Nordic Regulatory Specialist with over five years of experience in Regulatory Affairs within the Nordic pharmaceutical industry. The role involves managing regulatory activities across multiple Nordic countries, including compliance, quality assurance, and pharmacovigilance

Job Summary

  • Lead Regulatory Affairs activities as the Nordic Subject Matter Expert, including maintenance of Marketing Authorizations, preparation and submission of variations, lifecycle management, and coordination with Global and Nordic Regulatory colleagues.
  • You will be part of a dedicated team of three Regulatory experts working within the Nordics Cluster (Denmark, Finland, Iceland, Norway and Sweden), reporting to the Head of RQS – Nordics.
  • By joining our International Pharma Science Center (IPC) in Kastrup, you become part of Ferring’s global network—collaborating across functions in a state-of-the-art waterfront building with stunning views of Sweden and easy access to Copenhagen Airport.

Matching Summary

Match Score: 85

Ferring Pharmaceuticals is seeking a Nordic Regulatory Specialist with over five years of experience in Regulatory Affairs within the Nordic pharmaceutical industry. The role involves managing regulatory activities across multiple Nordic countries, including compliance, quality assurance, and pharmacovigilance.

Skills & Requirements

Must-have

  • Nordic pharmaceutical industry experience
  • Regulatory Affairs management
  • Marketing Authorizations maintenance
  • Promotional compliance and GDPR
  • Nordic regulatory systems maintenance

Nice-to-have

  • Collaborating with cross-functional teams
  • Navigating ambiguity with agility
  • Delivering clear presentations
  • International dynamic collaborative environment

Key Requirements

  • 5+ years' experience in pharmaceutical industry
  • Strong expertise in Regulatory Affairs
  • Experience in Pharmacovigilance, Quality Assurance
  • Fluent in English and at least one Nordic language

Work Rights

Candidates must be located in the Øresund region

Tailored Resume

Cover Letter